Canonical Allele Identifier: CA1268336309

Linked Data

dbSNP Id: rs1675138583

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.88859828_88859841del , CM000664.2:g.88859828_88859841del GRCh38
NC_000002.11:g.89159340_89159353del , CM000664.1:g.89159340_89159353del GRCh37
NC_000002.10:g.88940455_88940468del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000377423.6:c.388+2046_388+2059del (IGKV1-12) ENSP00000480537.2:n.388+2046_388+2059del
ENST00000430694.5:c.37+1046_37+1059del (IGKC) ENSP00000481923.2:n.37+1046_37+1059del
ENST00000610638.3:c.397+1685_397+1698del (IGKC) ENSP00000484499.3:n.397+1685_397+1698del
ENST00000634828.1:c.382+1685_382+1698del (IGKV1-8) ENSP00000489500.1:n.382+1685_382+1698del